Jerome I. Rotter

ORCID: 0000-0001-7191-1723
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About
Contact & Profiles
Research Areas
  • Genetic Associations and Epidemiology
  • Epigenetics and DNA Methylation
  • Nutrition, Genetics, and Disease
  • Inflammatory Bowel Disease
  • Liver Disease Diagnosis and Treatment
  • RNA modifications and cancer
  • Bioinformatics and Genomic Networks
  • Genetic Mapping and Diversity in Plants and Animals
  • Diabetes and associated disorders
  • Diabetes, Cardiovascular Risks, and Lipoproteins
  • Metabolomics and Mass Spectrometry Studies
  • Lipoproteins and Cardiovascular Health
  • Lipid metabolism and disorders
  • Pancreatic function and diabetes
  • Birth, Development, and Health
  • Genetic and phenotypic traits in livestock
  • Genomics and Rare Diseases
  • Cancer-related molecular mechanisms research
  • Adipokines, Inflammation, and Metabolic Diseases
  • Diet and metabolism studies
  • Cardiovascular Function and Risk Factors
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Helicobacter pylori-related gastroenterology studies
  • Retinal Diseases and Treatments
  • Cancer, Lipids, and Metabolism

University of California, Los Angeles
2016-2025

Harbor–UCLA Medical Center
2016-2025

The Lundquist Institute
2016-2025

UCLA Medical Center
2016-2025

Los Angeles Medical Center
2015-2024

University of Alabama at Birmingham
2007-2024

University of South Dakota
2023-2024

University of Cambridge
2016-2024

Johns Hopkins Medicine
2006-2024

Johns Hopkins University
2006-2024

The inflammatory bowel diseases Crohn's disease and ulcerative colitis are common, chronic disorders that cause abdominal pain, diarrhea, gastrointestinal bleeding. To identify genetic factors might contribute to these disorders, we performed a genome-wide association study. We found highly significant between the IL23R gene on chromosome 1p31, which encodes subunit of receptor for proinflammatory cytokine interleukin-23. An uncommon coding variant (rs11209026, c.1142G>A, p.Arg381Gln)...

10.1126/science.1135245 article EN Science 2006-10-27
Verneri Anttila Brendan Bulik‐Sullivan Hilary K. Finucane Raymond K. Walters José Brás and 95 more Laramie E. Duncan Valentina Escott‐Price Guido J. Falcone Padhraig Gormley Rainer Malik Nikolaos A. Patsopoulos Stephan Ripke Zhi Wei Dongmei Yu Phil H. Lee Patrick Turley Benjamin Grenier‐Boley Vincent Chouraki Yoichiro Kamatani Claudine Berr Luc Letenneur Didier Hannequin Philippe Amouyel Anne Boland Jean‐François Deleuze Emmanuelle Duron Badri N. Vardarajan Christiane Reitz Alison Goate Matthew J. Huentelman M. Ilyas Kamboh Eric B. Larson Ekaterina Rogaeva Peter St George‐Hyslop Hákon Hákonarson Walter A. Kukull Lindsay A. Farrer Lisa L. Barnes Thomas G. Beach F. Yesim Demirci Elizabeth Head Christine M. Hulette Gregory A. Jicha John S.K. Kauwe Jonathan Kaye James B. Leverenz Allan I. Levey Andrew P. Lieberman V. Shane Pankratz Wayne W. Poon Joseph F. Quinn Andrew J. Saykin Lon S. Schneider Amanda Smith Joshua A. Sonnen Robert A. Stern Vivianna M. Van Deerlin Linda J. Van Eldik Denise Harold Giancarlo Russo David C. Rubinsztein Antony Bayer Magda Tsolaki Petroula Proitsi Nick C. Fox Harald Hampel Michael J. Owen Simon Mead Peter Passmore Kevin Morgan Markus M. Nöthen Jonathan M. Schott Martin N. Rossor Michelle K. Lupton Per Hoffmann Johannes Kornhuber Brian Lawlor Andrew McQuillin Ammar Al‐Chalabi Joshua C. Bis Agustı́n Ruiz Merçé Boada Sudha Seshadri Alexa Beiser Kenneth Rice Sven J. van der Lee Philip L. De Jager Daniel H. Geschwind Markus J. Riemenschneider Steffi G. Riedel‐Heller Jerome I. Rotter Gerhard Ransmayr Bradley T. Hyman Carlos Cruchaga Montserrat Alegret Bendik S. Winsvold Priit Palta Kai-How Farh Ester Cuenca-León Nicholas A. Furlotte

Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We quantified genetic sharing 25 disorders from genome-wide association studies 265,218 patients 784,643 control participants assessed relationship to 17 phenotypes 1,191,588 individuals. Psychiatric common variant risk, whereas neurological appear more distinct one another psychiatric disorders. also identified significant between a number...

10.1126/science.aap8757 article EN Science 2018-06-21

The intestinal microflora, typically equated with bacteria, influences diseases such as obesity and inflammatory bowel disease. Here, we show that the mammalian gut contains a rich fungal community interacts immune system through innate receptor Dectin-1. Mice lacking Dectin-1 exhibited increased susceptibility to chemically induced colitis, which was result of altered responses indigenous fungi. In humans, identified polymorphism in gene for (CLEC7A) is strongly linked severe form...

10.1126/science.1221789 article EN Science 2012-06-07

Background Mild retinopathy (microaneurysms or dot-blot hemorrhages) is observed in persons without diabetes hypertension and may reflect microvascular disease other organs. We conducted a genome-wide association study (GWAS) of mild diabetes. Methods A working group agreed on phenotype harmonization, covariate selection analytic plans for within-cohort GWAS. An inverse-variance weighted fixed effects meta-analysis was performed with GWAS results from six cohorts 19,411 Caucasians. The...

10.1371/journal.pone.0054232 article EN cc-by PLoS ONE 2013-02-05

Background— The primary aim of genome-wide association studies is to identify novel genetic loci associated with interindividual variation in the levels risk factors, degree subclinical disease, or clinical disease. requirement for large sample sizes and importance replication have served as powerful incentives scientific collaboration. Methods— Cohorts Heart Aging Research Genomic Epidemiology Consortium was formed facilitate meta-analyses opportunities among multiple population-based...

10.1161/circgenetics.108.829747 article EN Circulation Cardiovascular Genetics 2009-02-01
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